172482462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71666305-C-T

172482954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71666796-G-A

172482954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71666796-G-C

172482994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71666818-G-A

172483405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667610-A-G

172483447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667645-G-A

172483731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667896-G-T

172484437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668291-G-C

172484459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668313-G-A

172484515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668370-G-A

172484732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668559-T-C

172484747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668572-T-C

172484767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668593-T-A

172484822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71668652-A-G

172484922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71668752-G-A

http://identifiers.org/hco/2/GRCh38#172484963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71668793-C-A

172484963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668793-C-G

172485191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71668992-G-A

172485191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71668992-G-C

172485191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71668992-G-T

172485192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71668993-T-A

172485248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71669049-A-G

172485399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71669300-G-A

172485511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71669429-G-A

http://identifiers.org/hco/2/GRCh38#172485515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71669433-C-A

172485776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71669644-C-T

172486100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71670164-C-T

172486371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71670380-G-A

172486655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71670613-G-C

172486881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71670821-G-A

172486881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71670821-G-T

172487080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71670963-C-T

http://identifiers.org/hco/2/GRCh38#172487358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71671224-A-C

172487509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71671373-A-G

172487526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71671390-T-C

172487591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71671455-T-A

172487626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71671490-C-T

172487672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71671532-A-G

172488166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71672028-G-A

http://identifiers.org/hco/2/GRCh38#172488225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71672087-C-A

http://identifiers.org/hco/2/GRCh38#172488277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71672159-C-A

172488277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71672159-C-G

172488277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71672159-C-T

172488330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71672240-T-C

172488400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71672413-T-G

http://identifiers.org/hco/2/GRCh38#172488405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71672418-C-A

172488481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71672542-C-T

172488558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71672623-T-C

172488643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71672702-C-G

172489148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673157-G-A

172489148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673157-G-T

http://identifiers.org/hco/2/GRCh38#172489353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71673349-A-C

172489353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673349-A-G

172489458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673446-G-T

172489628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71673616-A-G

172489731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673732-T-A

172489731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673732-T-G

172489802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673801-A-G

172489889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673872-G-A

172489889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673872-G-T

172489989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673964-G-A

172489989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71673964-G-T

172490186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71674112-G-A

http://identifiers.org/hco/2/GRCh38#172490677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71675070-C-A

172490755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71675161-G-A

172490755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71675161-G-T

172490942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71676064-G-A

172490942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71676064-G-T

172490997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71676103-A-G

http://identifiers.org/hco/2/GRCh38#172491047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71676150-A-C

172491047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71676150-A-G

172491169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71676272-G-C

172491169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71676272-G-T

172491202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71676304-T-G

172491298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71676394-G-A

172491300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71676396-G-A

http://identifiers.org/hco/2/GRCh38#172491301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71676397-C-A

172491301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71676397-C-T

172491380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71676464-T-G

http://identifiers.org/hco/2/GRCh38#172491458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71676541-A-C

172491685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71676758-G-A

172494554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678156-G-A

172494629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678226-C-G

172494629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678226-C-T

172494993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678517-C-G

172495110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678621-T-C

172495148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678651-T-G

172495170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678673-G-T

172495248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678751-T-C

172495307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71678809-A-G

172496833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71678884-G-A

172496936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71678976-G-T

172496976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71678999-G-A

172497087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679100-T-A

172497780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679526-G-C

http://identifiers.org/hco/2/GRCh38#172497798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71679543-A-C

172497824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679572-A-T

172497835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679582-T-G

172497914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679669-A-T

172497948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679702-A-G

http://identifiers.org/hco/2/GRCh38#172498107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71679857-C-A

172498107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71679857-C-T

172498144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679890-C-T

http://identifiers.org/hco/2/GRCh38#172498179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71679929-C-A

172498179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679929-C-G

172498179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71679929-C-T

172498244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71680238-G-C

172498277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71680268-C-T

172498299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71680287-T-C

172498362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71680357-A-G

172498444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71680442-G-C

172498457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71680454-T-A

http://identifiers.org/hco/2/GRCh38#172498707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71680698-A-C

172499161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71681117-T-C

172500545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71682048-G-C

172500547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71682050-G-T

172500842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71682353-T-G

http://identifiers.org/hco/2/GRCh38#172500874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71682380-A-C

172500874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71682380-A-G

http://identifiers.org/hco/2/GRCh38#172500930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71682434-A-C

172501067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71683244-C-G

172501067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71683244-C-T

172501272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71683445-G-A

172501708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71683814-G-A

172501708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71683814-G-T

172501716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71683822-G-C

172501716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71683822-G-T

172501724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71683830-C-T

172501846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71683952-A-G

172502315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71684425-A-G

172502450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71684563-C-T

172502684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71684795-A-G

172503557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685667-G-A

172503568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685678-T-A

172503577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685687-G-T

172503588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685698-G-A

172503588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685698-G-T

172503636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685733-T-G

172503713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685808-G-A

172503713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685808-G-T

172503793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685923-G-A

172503793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71685923-G-T

http://identifiers.org/hco/2/GRCh38#172503794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71685924-C-A

http://identifiers.org/hco/2/GRCh38#172503979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71686083-C-A

172503979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71686083-C-T

172504127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686234-G-A

172504127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686234-G-T

172504141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 71686248-T-C

172504141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 71686248-T-G

http://identifiers.org/hco/2/GRCh38#172504153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71686260-C-A

172504153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686260-C-T

172504237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686344-T-C

172504237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686344-T-G

http://identifiers.org/hco/2/GRCh38#172504253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71686362-C-A

172504253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686362-C-G

172504253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686362-C-T

http://identifiers.org/hco/2/GRCh38#172504422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71686535-C-A

http://identifiers.org/hco/2/GRCh38#172504511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71686624-C-A

172504511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686624-C-T

http://identifiers.org/hco/2/GRCh38#172504645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71686725-C-A

172504645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686725-C-T

172504810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686883-G-A

http://identifiers.org/hco/2/GRCh38#172504859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71686931-C-A

172504859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686931-C-T

172504900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71686972-T-C

172505026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687091-A-G

172505026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687091-A-T

http://identifiers.org/hco/2/GRCh38#172505049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71687119-C-A

172505237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687309-G-A

172505306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687375-C-T

172505400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687464-C-G

172505400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687464-C-T

172505410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687532-G-T

http://identifiers.org/hco/2/GRCh38#172505447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71687568-C-A

172505531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687679-G-A

172505531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71687679-G-T

172505764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71688137-C-T

172505771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71688145-C-T

http://identifiers.org/hco/2/GRCh38#172505932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71688319-C-A

172506453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71689352-C-G

172506557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71689453-C-T

172506617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71689503-G-C

http://identifiers.org/hco/2/GRCh38#172506971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71689783-A-C

172507323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71690080-T-G

172508037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71690442-G-A

172508565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71691570-T-C

172508891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71691899-C-T

172508901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71691908-A-G

172553978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71698536-G-A

172554039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71698584-C-T

172555512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703169-T-C

http://identifiers.org/hco/2/GRCh38#172555705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71703306-A-C

172555705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703306-A-G

172555776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703361-T-C

172555776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703361-T-G

172555814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703402-G-A

172555814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703402-G-T

http://identifiers.org/hco/2/GRCh38#172555864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71703432-C-A

172555864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703432-C-G

172555864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703432-C-T

172555903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703471-G-A

http://identifiers.org/hco/2/GRCh38#172555908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71703486-C-A

172555908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703486-C-T

172555940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703520-G-A

172555940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703520-G-C

172555940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703520-G-T

172556014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703573-T-A

172556014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703573-T-C

172556014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703573-T-G

172556018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703577-G-A

172556018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703577-G-C

172556018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703577-G-T

172556074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703632-A-G

172556114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703676-T-C

http://identifiers.org/hco/2/GRCh38#172556359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71703924-C-A

172556359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703924-C-G

172556359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703924-C-T

172556444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703960-T-A

172556444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703960-T-C

172556444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71703960-T-G

http://identifiers.org/hco/2/GRCh38#172556458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71703974-C-A

http://identifiers.org/hco/2/GRCh38#172556525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71704043-C-A

172556525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71704043-C-T

172556570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71704112-T-A

172556570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71704112-T-C

http://identifiers.org/hco/2/GRCh38#172556581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71704123-C-A

172556581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71704123-C-T